Top 1324 Sr development editor Jobs

Senior Non-Clinical Editor
Kaztronix —Wilmington, DE
- Contract
- Remote
- Microsoft Word
- Microsoft Excel
- Writing skills
Quick Apply
1d
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ISTE+ASCD —Arlington, VA
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Senior Managing Editor, Content and Test Development
Cambium Learning Group —Remote
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Scholastic —New York, NY
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Macmillan Publishers —New York, NY
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Sr. Editor - Station Engagement
Minnesota Public Radio —Saint Paul, MN
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- 5 years
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The Lawfare Institute —Washington, DC
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Associate Tech Editor, Lifehacker
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Editor-in-Chief, SUCCESS Magazine - (REMOTE)
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Deloitte —Houston, TX
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Benchmark Education Company LLC —New Rochelle, NY
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Managing Editor
The Aspen Institute —Washington, DC
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- Full-time
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Senior Content Editor
C2 Technologies —Arlington, VA
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Sr Enhancement Specialist Editor (DXC)
BAE Systems Inc. —Springfield, VA
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- Full-time
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- English
- Research
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- Paid holidays

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Senior Non-Clinical Editor

Kaztronix -
Wilmington, DE

Quick Apply

Job Details

Contract
1 day ago

Qualifications

Microsoft Word
Communication with suppliers
Microsoft Excel
Presentation software
Clinical development
Writing skills
Word embeddings
Visio
Pharmaceutical company experience
Vendor relationship management
Vendor communication
Content publishing

Full Job Description

Job Summary
This position is responsible for overall quality control (QC) review and submission-ready publishing of nonclinical documents. The Senior Nonclinical Editor will copyedit/proofread, format, and perform internal consistency review of document content in accordance with company SOPs and processes to ensure documents meet required standards. This role will support all documents written by authors from Drug Metabolism and Biopharmaceutics (DMB), Chemistry Manufacturing and Controls (CMC), Toxicology (Tox), and Translational Sciences. This position may also assist in clinical document QC and publishing tasks when appropriate to meet submission timelines. The Senior Nonclinical Editor performs the activities with minimal oversight needed.

Summary of the Essential Functions of the Job

Perform internal document QC review of nonclinical documents (eg, DMB, CMC, TOX, TRS, PRECLIN) to ensure compliance with the Style Guide, template formatting, and submission ready standards.
Copyedit/proofread for grammar, style, and formatting according to AMA and style guides.
Ensure internal consistency and confirm that data are reported correctly, statements accurately reflect a common message and text to tables, figures, and appendices are accurate and consistently presented.
Check the reference list in documents, including verifying citation information via PubMed, ordering copies of references, and adding to the electronic document management system (EDMS), and ensuring each reference is cross-referenced in the document.
Proofread documents against the standard templates to ensure compliance with required sections and text.
Perform publishing of PDF documents to submission-ready standards. May involve multiple document compilation of PDF files to include appendices.
Assist Medical Writing Operations staff with clinical document QC and publishing, as appropriate.
Participate in process improvement initiatives and support Medical Writing staff with other tasks, as appropriate.
May interact cross-functionally to support clinical and nonclinical processes and template updates.

Minimum Requirements

Bachelor s degree in English, Basic Science, Business, or other analytical field with 4 years related experience in the pharmaceutical industry OR 8+ years of experience in a discipline directly related to document production (eg, medical writing, QC, editing, publishing).
Strong working knowledge of the editorial and publishing activities within Clinical Development.
Proficient in Microsoft Word, including the ability to format tables, insert cross-references, apply styles, and use templates. Experience with PowerPoint, Excel, Visio, Adobe.
Strong working knowledge of Adobe PDF bookmarking and internal/external hyperlinking to meet submission-ready standards.
Experience in the use of an EDMS (eg, Veeva Vault or SharePoint).
Ability to effectively communicate with vendors and manage outsourced editorial work.
Keen attention to detail.
Ability to manage multiple activities, prioritize effectively, and work in a fast-paced, deadline-driven environment.
Strong organizational and time management skills.
Strong verbal, written, and interpersonal communication skills.

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.

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Refine Your Search

sr development editor jobs

Senior Non-Clinical Editor

Copy Editor

Editor, Editorial – Development

Senior Managing Editor

Senior Research Scientist (Prof Haidt)

Senior Editor

Senior Editor

Sr. Editor

Senior Managing Editor, Content and Test Development

Senior Editor

Associate Editor

Sr. Editor - Station Engagement

Associate Editor

Associate Tech Editor, Lifehacker

Editor-in-Chief, SUCCESS Magazine - (REMOTE)

Editor, Consumer Industry

Senior Content Developer

Managing Editor

Senior Content Editor

Sr Enhancement Specialist Editor (DXC)

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